Our mission is to improve the health prospects of women living with
lymphangioleio​myomatosis (LAM).

LAM Australia Research Alliance is a not-for-profit organisation run wholly by volunteers.

ABOUT US

  • Funding research to find a cure for LAM
  • Raising awareness of LAM
  • Supporting women living with LAM

DOCTORS WITH LAM EXPERTISE

PATIENT SUPPORT CONTACTS FOR WOMEN NEWLY DIAGNOSED WITH LAM

NEWS

Please join us for the Annual General Meeting on Tuesday 11 August 2020 at 18.00 AEST. Our AGM will be followed by a talk by Prof Allan Glanville, world clinical authority on the treatment of LAM. Our talk will be held on Zoom. If you have not received an email already about the AGM, pleased email us at admin@lamaustralaia.org.au to register.

RESEARCH GIVES HOPE TO WOMEN WITH LAM